HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396071Generated: November 1, 2026
Azobisisobutyronitrile → 2-Oxazolidinone, 3-acetyl-5-chloro-
https://huagongshe.com/reaction/1396071
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 3-Acetyl-2-oxazolidinone | HCID 538766 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Oxazolidinone, 3-acetyl-5-chloro- | HCID 12289576 | — |
Reaction Steps
5.00 g of 3-acetyloxazolidin-2-one were initially charged in 25 ml of carbon tetrachloride and heated to 70° C. under an argon atmosphere. Then, alternately, a solution of 3.46 ml of sulfuryl chloride in 5 ml of carbon tetrachloride and 0.10 g of 2,2′-azobis(2-methylpropionitrile) were added, and then the mixture was stirred at the same temperature for 2 hours. After cooling to room temperature, the clear solution was decanted off from the solid residues, and the solvent was removed under reduced pressure. This gave the product (6.80 g) with a molecular weight of 163.6 g/mol (C5H6ClNO3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901114B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-a4b3da96da004f8a8730862dbe3bce08 |
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| Source note | uspto-grants-2014_12 |
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